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The collagen superfamily and collage...
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Ruggiero, Florence.
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The collagen superfamily and collagenopathies
紀錄類型:
書目-電子資源 : Monograph/item
正題名/作者:
The collagen superfamily and collagenopathies/ edited by Florence Ruggiero.
其他作者:
Ruggiero, Florence.
出版者:
Cham :Springer International Publishing : : 2021.,
面頁冊數:
ix, 338 p. :ill., digital ;24 cm.
內容註:
Chapter 1: Introduction to the collagen superfamily -- Chapter 2: Collagen IV-related disease -- Chapter 3: Articular collagens related diseases -- Chapter 4: Collagens as new players of nervous system disease -- Chapter 5: Collagens and EDS -- Chapter 6: Collagens and dystrophic epidermolysis bullosa -- Chapter 7: Collagen-related myopathies: pathogenic mechanisms and prospective therapies -- Chapter 8: Procollagen trafficking and its implicaitons in Osteogenesis Imperfecta.
Contained By:
Springer Nature eBook
標題:
Collagen. -
電子資源:
https://doi.org/10.1007/978-3-030-67592-9
ISBN:
9783030675929
The collagen superfamily and collagenopathies
The collagen superfamily and collagenopathies
[electronic resource] /edited by Florence Ruggiero. - Cham :Springer International Publishing :2021. - ix, 338 p. :ill., digital ;24 cm. - Biology of extracellular matrix,v.80887-3224 ;. - Biology of extracellular matrix ;v.8..
Chapter 1: Introduction to the collagen superfamily -- Chapter 2: Collagen IV-related disease -- Chapter 3: Articular collagens related diseases -- Chapter 4: Collagens as new players of nervous system disease -- Chapter 5: Collagens and EDS -- Chapter 6: Collagens and dystrophic epidermolysis bullosa -- Chapter 7: Collagen-related myopathies: pathogenic mechanisms and prospective therapies -- Chapter 8: Procollagen trafficking and its implicaitons in Osteogenesis Imperfecta.
This book aims at providing insights into the collagen superfamily and the remarkable diversity of collagen function within the extracellular matrix. Additionally, the mechanisms underlying collagen-related diseases such as dystrophic epidermolysis bullosa, osteogenesis imperfecta, as well as collagen-related myopathies and neurological disorders are discussed. Collagens are the most abundant extracellular matrix proteins in organisms. Their primary function is to provide structural support and strength to cells and to maintain biomechanical integrity of tissues. However, collagens can no longer be considered just as structural proteins. They can act as extracellular modulators of signaling events and serve critical regulatory roles in various cell functions during embryonic development and adult homeostasis. Furthermore, collagens are associated with a broad spectrum of heritability-related diseases known as "collagenopathies" that affect a multitude of organs and tissues including sensorial organs. The book is a useful introduction to the field for junior scientists, interested in extracellular matrix research. It is also an interesting read for advanced scientists and clinicians working on collagens and collagenopathies, giving them a broader view of the field beyond their area of specialization.
ISBN: 9783030675929
Standard No.: 10.1007/978-3-030-67592-9doiSubjects--Topical Terms:
892448
Collagen.
LC Class. No.: QP552.C6 / C65 2021
Dewey Class. No.: 572.67
The collagen superfamily and collagenopathies
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Chapter 1: Introduction to the collagen superfamily -- Chapter 2: Collagen IV-related disease -- Chapter 3: Articular collagens related diseases -- Chapter 4: Collagens as new players of nervous system disease -- Chapter 5: Collagens and EDS -- Chapter 6: Collagens and dystrophic epidermolysis bullosa -- Chapter 7: Collagen-related myopathies: pathogenic mechanisms and prospective therapies -- Chapter 8: Procollagen trafficking and its implicaitons in Osteogenesis Imperfecta.
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This book aims at providing insights into the collagen superfamily and the remarkable diversity of collagen function within the extracellular matrix. Additionally, the mechanisms underlying collagen-related diseases such as dystrophic epidermolysis bullosa, osteogenesis imperfecta, as well as collagen-related myopathies and neurological disorders are discussed. Collagens are the most abundant extracellular matrix proteins in organisms. Their primary function is to provide structural support and strength to cells and to maintain biomechanical integrity of tissues. However, collagens can no longer be considered just as structural proteins. They can act as extracellular modulators of signaling events and serve critical regulatory roles in various cell functions during embryonic development and adult homeostasis. Furthermore, collagens are associated with a broad spectrum of heritability-related diseases known as "collagenopathies" that affect a multitude of organs and tissues including sensorial organs. The book is a useful introduction to the field for junior scientists, interested in extracellular matrix research. It is also an interesting read for advanced scientists and clinicians working on collagens and collagenopathies, giving them a broader view of the field beyond their area of specialization.
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